Making way for suppressing the FGF19/FGFR4 axis in cancer

Future Med Chem. 2018 Oct;10(20):2457-2470. doi: 10.4155/fmc-2018-0099. Epub 2018 Oct 16.

Abstract

FGF19 is a noncanonical FGF ligand that can control a broad spectrum of physiological responses, which include bile acid homeostasis, liver metabolism and glucose uptake. Many of these responses are mediated by FGF19 binding to its FGFR4/β-klotho receptor complex and controlling activation of an array of intracellular signaling events. Overactivation of the FGF19/FGFR4 axis has been implicated in tumorigenic formation, progression and metastasis, and inhibitors of this axis have recently been developed for single agent use or in combination with other anticancer drugs. Considering the critical role of this receptor complex in cancer, this review focuses on recent developments and applications of FGF19/FGFR4-targeted therapeutics.

Keywords: FGF19; FGFR4; anticancer; inhibitors; oncogenic role; signaling transduction; treatment regimens.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / metabolism*
  • Bile Acids and Salts / metabolism
  • Carcinogenesis / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Fibroblast Growth Factors / genetics
  • Fibroblast Growth Factors / metabolism*
  • Humans
  • Klotho Proteins
  • Membrane Proteins / metabolism
  • Molecular Targeted Therapy / methods
  • Protein Binding
  • Receptor, Fibroblast Growth Factor, Type 4 / metabolism*
  • Signal Transduction

Substances

  • Antineoplastic Agents
  • Bile Acids and Salts
  • FGF19 protein, human
  • KLB protein, human
  • Membrane Proteins
  • Fibroblast Growth Factors
  • FGFR4 protein, human
  • Receptor, Fibroblast Growth Factor, Type 4
  • Klotho Proteins